Drug recall
Atrium Firm PVC Thoracic Catheter 28French-Intended to facilitate the evacuation of air and/or fluid from the…
FDA recall event 90295 · Class II · Atrium Medical Corporation
Key facts
| Event ID | 90295 |
|---|---|
| Recall numbers | Z-1297-2022 |
| Recalling firm | Atrium Medical Corporation |
| Product type | Devices |
| Products | Atrium Firm PVC Thoracic Catheter 28French-Intended to facilitate the evacuation of air and/or fluid from the chest cavity or mediastinum. Product REF Number: 15028 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mismatch between the expiration date on the sterile barrier pouch and the expiration date on the case/shipper label. Product sterile barrier pouch label expiration date of 16SEP2024 (2024-09-16) while… |
| Initiation date | Apr 21, 2022 |
| Report date | Jul 6, 2022 |
| City | Merrimack |
| State | NH |
| Country | United States |
| FEI number | 3011175548 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: